BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    SELECT-A-FLOW COLLECTOR

    K Number: K810645 · Decision May 5, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    127
    Registration Numbers
    127
    Same Product Code
    205
    Applicant Total
    2
    Review Days
    56

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    Basic Information

    Device Name
    SELECT-A-FLOW COLLECTOR
    K Number
    K810645
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5250
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Wenmar Intl. Corp.
    Date Received
    March 10, 1981
    Decision Date
    May 5, 1981
    Product Code
    KNX
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    KNX Collector, Urine, (And Accessories) For Indwelling Catheter

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    Other Clearances by Wenmar Intl. Corp.

    K Number Device Name
    K811857 SELECT-A-FLOW